responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment
engagement activities
preparation, packing, and dispatching of kits for clinical trials conducted by WDIH
Adaptable and reliable
incumbent will be responsible for: Didactic and clinical / experiential training of undergraduate and postgraduate Three years' appropriate veterinary experience (clinical, research, industry or regulatory dealing largely
incumbent will be responsible for: Didactic and clinical / experiential training of undergraduate and postgraduate Three years' appropriate veterinary experience (clinical, research, industry or regulatory dealing largely